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| Company | IBL-America | IBL-America | IBL-America | IBL-America | IBL-America |
| Item | Endothelial Lipase (EL) C-Terminal ELISA | BACE1 ELISA Assay | Bevacizumab (Avastin®) ELISA | Epstein-Barr Virus (EBNA-1) IgM ELISA | Progesterone ELISA Assay |
| Citations | | | | | |
| Catalog Number | 27263 | 27752 | TM09010 | IB79860 | IB79105 |
| Price | Supplier Page | Supplier Page | Supplier Page | Supplier Page | Supplier Page |
| Description | Solid phase sandwich enzyme-linked immunosorbent assay (ELISA) for the determination of Endothelial Lipase (EL) C-Terminal in human serum and EDTA-plasma. For research use only, not for use in diagnostic procedures. | Solid phase sandwich ELISA for the determination of BACE1 in human, mouse or rat brain extracts or cultured cell lysate. For research use only, not for use in diagnostic procedures. | Enzyme immunoassay (ELISA) test kit for the determination of free antibodies directed against the drug Bevacizumab (Avastin®) in serum and plasma. For research use only, not for use in diagnostic procedures. | Enzyme immunoassay for the determination of IgM-class antibodies to Epstein-Barr virus nuclear-1 antigen (EBV-EBNA-1) in human serum or plasma. For research use only - not for use in diagnostic procedures. | Enzyme immunoassay (ELISA) for the quantitative determination of Progesterone in serum and plasma. FDA exempt, can be used for in-vitro diagnostics. |
| Detection Target | Noradrenaline | CA 72-4 | Bevacizumab (Avastin®) | Schistosoma mansoni IgG | Adrenaline / Noradrenaline |
| Sample Type | Multiple | Serum, Blood Plasma | Serum and plasma. | Serum, Blood Plasma | Multiple |
| Method | Enzyme-Linked Immunosorbent Assay (ELISA) | Enzyme-Linked Immunosorbent Assay (ELISA) | Enzyme-Linked Immunosorbent Assay (ELISA) | Enzyme-Linked Immunosorbent Assay (ELISA) | Enzyme-Linked Immunosorbent Assay (ELISA) |
| Detection Range | 0 / 0.13 to 8 ng/mL | 1.56 to 100 ng/mL | 0 / 6 to 200 ng/mL | A cut-off control is used for the interpretation of results. | 0.3 to 40 ng/mL |
| Sensitivity | 0.1 ng/mL x Correction Factor (please see protocol) | 0.79 U/mL | 2 ng/mL | 93.75% (95% confidence interval: 82.8% - 98.69%) | Adrenaline: 0.25 ng/mL x C*; Noradrenaline: 0.1 ng/mL x C*. Sensitivity based on calculated correction factor. |
| Assay Time | Overnight + 30 min. (incubation) | 2 hrs (incubation) | 1 hour, 45 min. total incubation time. | 1 hr 45 mins (incubation) | 1 hr 20 mins (incubation) |
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